O-alkyl(-cycloalkyl)-s-alkyl-s-phenyl-phosphorodithiolates

ABSTRACT

O-ALKYL(-CYCLOALKYL)-S-ALKYL - S - PHENYL-PHOSPHORODITHIOLATES, I.E. O-ALKYL AND CYCLOALKYL-S-ALKYL-S-(OPTIONALLY CHLORO AND METHYL-SUBSTITUTED)-PHENYL - PHOSPHORODITHIOLATES OR -DITHIOLPHOSPHATES, WHICH POSSESS FUNGICIDAL PROPERTIES.

United States Patent O 3,784,654 -ALKYL(-CYCLOALKYLyS-ALKYL-S-PHENYL- PHOSPHORODITHIOLATES Toyohiko Kume and Kazuomi Yasni, Tokyo, Japan, assignors to Bayer Aktiengesellschaft, Leverkusen, Germany No Drawing. Filed June 3, 1969, Ser. No. 830,153 Claims priority, application Japan, June 18, 1968, 43/41,618 Int. Cl. A0111 9/36; C071? 9/16 US. Cl. 260-958 11 Claims ABSTRACT OF THE DISCLOSURE O-alkyl(-cycloalkyD-S-alkyl S phenyl-phosphorodithiolates, i.e. O-alkyl and cycloalkyl-S-alkyl-S-(optionally chloro and methyl-substituted)-phenyl phosphorodithiolates or -dithiolphosphates, which possess fungicidal properties.

The present invention relates to and has for its objects the provision for particular new O-alkyl(-cycloalkyl)-S- alkyl-S-ph enyl-phosphorodithiolates, i.e. O-alkyl and cycloalkyl-S-alkyLS-(optionally chloro and methyl-substituted) -phenyl- -phosphorodithiolates or -dithiolphosphates, which possess fungicidal properties, active compositions in the form of mixtures of such compounds with solid and liquid dispersible carrier vehicles, and methods for producing such compounds and for using such compounds in a new way especially for combating fungi, with other and further objects becoming apparent from a study of the within specification and accompanying examples.

Heretofore, in controlling serious rice diseases such as blast and sheath blight, organic mercury compounds and organic arsenic compounds such as phenyl mercuric acetate (A), methyl arsonic acid, salts, etc., which contain heavy metals harmful to man and cattle have been used widely, because they are excellent in their fungicidal effect and are comparatively economical to use. However, the use of organic mercuric compounds during the growing period of rice plants is objectionable from a public health standpoint because of the direct and indirect toxicity of these known compounds to mammals.

Accordingly, inexpensive and eifective compounds which do not contain any heavy metals harmful to man and cattle are urgently needed to combat rice diseases.

It has now been found, in accordance with the present invention, that the particular new O-alkyl(-cycloalkyl)-S-alkyl-S-phenyl-phosphorodithiolates of the formula in which R is alkyl of 1-4 carbon atoms,

R is alkyl of 1-6 carbon atoms or cycloalkyl of 5-6 ring carbon atoms, and

X is hydrogen, chloro or methyl,

exhibit strong fungicidal properties.

ice

in which R and R are the same as defined above, and Hal is a halogen atom such as chloro,

with a thiophenol of the formula X is the same as defined above, and M is hydrogen or alkali metal such as sodium.

Surprisingly, the particular new phosphorodithiolates of Formula I above according to the present invention exhibit an excellent fungitoxic effectiveness, especially for agricultural and horticultural purposes, more especially against rice diseases, and a certain insecticidal effectiveness, with a comparatively low mammalian toxicity and a concomitantly low phytotoxicity, whereas the known organic mercury and organic arsenic compounds used for these purposes as aforesaid are highly toxic to mammals. Therefore, the instant compounds represent a valuable contribution to the art.

The general process for the preparation of the instant compounds is illustrated by the following reaction scheme:

(III) in which The starting materials to be used for producing the instant new compounds are already known and are clearly characterized by the Formulae II and III noted above.

Advantageously, in accordance with the present invention, in the various formulae herein:

R represents lower alkyl hydrocarbon of 1-4 carbon atoms such as methyl, ethyl, n and iso-propyl, n-, iso-, sec.- and tert.-butyl, and the like, especially c or C alkyl;

R represents lower alkyl hydrocarbon of l-6 carbon atoms such as methyl, ethyl, nand iso-propyl, n-, iso-, sec.- and tert.-butyl, nand iso-amyl, nand iso-hexyl, and the like, especially C or C or C alkyl, and more especially n-butyl, nor iso-propyl or cycloalkyl hydrocarbon of -6 ring carbon atoms such as cyclopentyl, cyclohexyl, and the like, especially cyclohexyl;

X represents hydrogen; chloro; or methyl; X when chloro or methyl being in 2-, 3- or 4-position;

Hal represents halo such as chloro, bromo, fluoro and iodo, especially chloro; and

M represents, an alkali metal atom such as sodium, potassium, lithium, and the like, especially sodium and potassium.

As examples of thiolphosphoryl halides of Formulae II above which may be used as starting materials, there are mentioned: O-n-butyl-S-methyl-, O-n-butyl-S-ethyL, On-butyl-S-sec.-butyl-, O-n-hexyl-S-ethyl-, O-isopropyl- S-ethyl-, O-ethyl-S-methyl-, O-cyclohexyl-S-methyl-, O- cyclohexyl-S-ethyl-, O-cyclohexyl-S-n-butyl-, and the like, thiolphosphoryl chlorides, bromides, etc.

As examples of thiophenols and corresponding alkali metal salts of Formula III above which may be used as starting materials, there are mentioned: thiophenol, 2-, 3- and 4-chloro-thiophenol, 2-, 3- and 4-methyl-thiophenol, and the corresponding sodium and potassium thiophenates, and the like.

Suitable inert organic solvents usable for carrying out the production process in accordance with the present invention include hydrocarbons, such as benzene and benzine; chlorinated hydrocarbons, such as methylene chloride, ethylene chloride, carbon tetrachloride and dichlorobenzene; alcohols such as methanol, ethanol, propanol and butanol; ethers, such as diethyl ether, dibutyl ether and dioxan; ketones, such as acetone, cyclohexanone and methylethyl ketone; and acetonitrile and dimethyl formamide; and the like.

The reaction temperature can be varied within a fairly wide range. In general, the reaction is carried out at substantially between about 0-100 C., preferably between about 080 C.

A basic substance, preferably a tertiary amine, such as triethylamine, pyridine, dimethyl-cyclohexylamine, dimethylaniline and dimethylbenzylamine, is advantageously employed as acid binding agent Where the corresponding free starting thiophenol is used.

When carrying out the production process, approximately equimolar amounts of the starting reactants are used, but an excess of the acid binding agent is not harmful, i.e. Where the free thiophenol is used. An inert organic solvent such as benzene may be employed and the reaction may be carried out, for example in trimethylamine as acid binding agent, at a temperature of about 0-80 C., by dissolving the thiophenol and triethylamine in benzene and adding the thiolphosphoryl halide dropwise thereto.

After completion of the reaction (about 1-5 hours), the reaction mixture may be worked up in the usual manner, such as by washing the reaction mixture with water and thereafter with aqueous sodium carbonate solution and water, then drying with sodium sulfate, and distilling off the benzene. The residue is in the most cases a colorless or slightly yellow colored oil which is soluble in organic solvents and only slightly soluble in water.

Advantageously, the particular new active compounds according to the present invention exhibit strong fungitoxic activity and are distinguished by a broad spectrum of activity. Their low toxicity to warm-blooded animals and their good compatibility with higher plants permits the instant new compounds to be used as plant protection agents against fungal plant diseases. In the concentrations normally used for the control of fungi, the instant compounds do not damage cultivated plants.

Fungitoxic agents, such as the instant compounds, are usable in the plant protection, i.e. agricultural and horticultural endeavors, for the control of fungi from the most diverse classes of fungi such as Archimycetes, Phycomycetes, Asconycetes, Basidiomycestes and Fungi Imperfecti.

The particular new active compounds according to the present invention can be used for example against parasitic fungi, on above-the-soil parts of plants, fungi which cause tracheomycosis which attack the plant from the soil, seedborne fungi and soil-inhabiting fungi.

By reason of their excellent properties mentioned above, the particular new active compounds according to the present invention can also be used with good results against fungal diseases which hitherto had to be controlled with fungicidal agents containing heavy metals harmful to man and cattle, e.g. arsenic and mercury.

The instant active compounds have given particularly good results in the control of serious rice diseases including not only rice blast and brown spot, but also sheath blight. Thus, the instant compounds show an excellent activity against the fungi Pirz'cularia oryzae (i.e. blast), Cochliobolus miyabeanus (i.e. brown spot) and Pellicu- [aria sasalii (i.e. sheat blight), as well as against the fungi Mycosphaerella melonis (cucumber), Alternia kikuchiana (pear), Elsinoe ampelina (grape), and the like.

The active compounds according to the instant invention an be utilized, if desired, in the form of the usual formulations or compositions with conventional inert pesticidal diluents or extenders, i.e. inert conventional pesticidal dispersible carrier vehicles, such as solutions, emulsions, suspensions, emulsifiable concentrates, spray powder, pastes, soluble powders, dusting agents, granules, etc. These are prepared in known manner, for instance by extending the active compound with conventional pesticidal dispersible liquid diluent or carriers and/ or dispersible solid carriers optionally with the use of carrier vehicle assistants, e.g. conventional pesticidal surface-active agents, including emulsifying agents and/or dispersing agents, whereby, for example, in the case where water is used as diluent, organic solvents may be added as auxiliary solvents. The following may be chiefly considered for use as conventional carrier vehicles for this purpose: inert dispersible liquid diluent carriers including inert organic solvents and non-solvents, such as aromatic hydrocarbons (e.g. benzene, toluene, xylene, dimethyl naphthalene, aromatic naphthas, etc.), halogenated, especially chlorinated, aromatic hydrocarbons (e.g. chlorobenzenes, etc.), paraffins (e.g. petroleum fractions), chlorinated aliphatic hydrocarbons (e.g. methylene chloride, etc.), alcohols (e.g. methanol, ethanol, propanol, butanol, etc.), amines (e.g. ethanolamine, etc.), ethers, ether-alcohols (e.g. glycol monomethyl ether, etc.), amides (e.g. dimethyl formamide, etc.), sulfoxides (e.g. dimethyl sulfoxide, etc.), ketones (e.g. acetone, etc.), and/ or water; as well as inert dispersible finely divided solid carriers, such as ground natural minerals (e.g. kaolins, alumina, silica, chalk, i.e. calcium carbonate, talc, kieselguhr, diatomaceous earth, clay, montmorillonite, etc.), and ground synthetic minerals (e.g. highly dispersed silicic acid, silicates, e.g. alkali silicates, etc.); whereas the following may be chiefly considered for use as conventional carrier vehicle assistants, e.g. surface-active agents, for this purpose: emulsifying or wetting agents, such as nonionic and/or anionic emulsifying or wetting agent (e.g. polyethylene oxide esters of fatty acids, polyethylene oxide ethers of fatty alcohols, alkyl sulfonates, aryl sulfonates, etc., and especially alkyl aryl-polyglycol ethers, magnesium stearate, sodium oleate, etc.); and/or dispersing agents, such as lignin, sulfite waste liquors, methyl cellulose, etc.

Such active compounds may be employed alone or in the form of mixtures with one another and/ or with such solid and/or liquid dispersible carrier vehicles and/or with other known compatible active agents, especially plant protection agents, such as other fungicides, or herbicides, insecticides, acaricides, nematocides, bactericides, etc., including especially organo-phosphorus compounds, carbamate compounds, dithiocarbamate compounds, chlorine compounds, dinitro compounds, organic sulfur or copper compounds, substituted phenoxy compounds, chlorophenols, substituted diphenyl ethers, anilide compounds, uneas, triazines, antibiotics, and other known agricultural chemicals and/or fertilizers, if desired, or in the form of particular dosage preparations for specific application made therefrom, such as solutions, emulsions, suspensions, powders, pastes, and granules which are thus ready for use.

As concerns commercially marketed preparations, these generally contemplate carrier composition mixtures in which the active compound is present in an amount substantially between about 01-95%, and preferably 0.5- 90%, by weight of the mixture, whereas carrier composition mixtures suitable for direct application or field application generally contemplate those in which the active compound is present in an amount substantially between about 0.001-%, preferably 0.05-5%, by weight of the mixture. Thus, the present invention contemplates overall compositions which comprise mixtures of a conventional dispersible carrier vehicle such as (1) a dispersible inert finely divided carrier solid, and/or (2) a dispersible liquid such as an inert organic solvent and/or water preferably including a surface-active effective amount of a carrier vehicle assistant, e.g. a surface-active agent, such as an emulsifying agent and/or a dispersing agent, and an amount of the active compound which is effective for the purpose in question and which is generally about 0.00195%, and preferably ODS-95%, by weight of the mixture.

Generally, the active compound is used in dosage amounts per unit area of substantially between about 1000, preferably 40-600, and most preferably 40-100 g. per 10 ares, irrespective of the presence or absence of such carrier vehicle.

The active compounds can also be used in accordance with the well-known ultra-low-volume process with good success, i.e. by applying such compound if normally a liquid, or by applying a liquid composition containing the same, via very effective atomizing equipment in finely divided form, e.g. average particle diameter of from 50- 100 microns; or even less, i.e. mist form, for example by airplane crop spraying techniques. Only up to at most about a few liters/hectare are needed, and often amounts only up to about 1 quart/acre, preferably 2-16 fluid ounces/acre, are sufiicient. In this process it is possible to use highly concentrated liquid compositions with said liquid carrier vehicles containing from about to about 95% by weight of the active compound, or even the 100% active substance alone, e.g. about 20-100% by weight of the active compound.

In particular, the present invention contemplates methods of selectively killing, combating or controlling fungi, which comprise applying to at least one of (a) such fungi and (b) their habitat, i.e. the locus to be protected, a fungicidally effective or toxic amount of the particular active compound of the invention alone or together with a carrier vehicle as noted above. The instant formulations or compositions are applied in the usual manner, for instance by spraying, atomizing, vaporizing, scattering, dusting, watering, sprinkling, pouring, dressing, via incrustation; and the like.

Significantly, the fungicidal compositions of the present invention can be applied for example by spraying a dust formulation directly onto stems and leaves of plants; or by using the formulation for seed-dressing; by spraying an emulsifiable concentrate, diluted with water, etc. to a desirable concentration, onto stems and leaves of plants; by suspending a wettable powder in water at a desirable concentration and spraying the formulation onto stems and leaves of plants; by applying granule formulations to soil; and the like.

It will be realized, of course, that the concentration of the particular active compound utilized in admixture with the carrier vehicle will depend upon the intended application, the purpose for which the active compound is used, and the like. Therefore, in special cases, it is possible to go above or below the aforementioned concentration ranges and dosage amounts per unit area.

The following illustrate, without limitation, examples of formulations which may be used in accordance with the present invention:

FORMULATION A 15 parts of instant compound (3), parts of a mixture of diatomaceous earth and kaolin (1:5) and 5 parts of the emulsifier Runox (trade name of the product of Toyo Kagaku Kogyo K.K., Japan) polyonyethylenealkylarylether are formulated into a wettable powder by crushing and mixing. It is diluted with water at the concentration of 1 to 300-500 and applied by spraying to the phytopathogenic fungi and/ or their habitat.

FORMULATION B 30 parts of instant compound (7), 30 parts of xylene and 30 parts of Kawakazol (trade name of the product of Kawasaki Kasei Kogyo K.K., Japan) aromatic hydrocarbons of high boiling point and 10 parts of the emulsifier Sorpol (trade name of the product of Toho Kagaku Kagyo K.K., Japan); polyoxyethylene-alkylarylether are formulated into an emulsifiable concentrate by mixing and stirring. It is diluted with water at the concentration of 1 to 1.000 and applied by spraying to the phytopathogenie fungi and/ or their habitat.

FORMULATION C 2 parts of instant compound (8) and 98 parts of a mixture of talc and clay (3:1) are formulated into a dust by crushing and mixing. It is applied as is by dusting to the phytopathogenic fungi and/or their habitat.

FORMULATION D 1.5 parts of instant compound (3), 1.5 parts of O-ethyl- S,S-diphenyl-phosphorodithiolate, and 97 parts of a mixture of talc and clay (3:1) are formulated into a dust by crushing and mixing. It is applied in the same manner described in Formulation C.

The fungicidal effectiveness of the particular new compounds of the present invention is illustrated, without limitation, by the following examples:

EXAMPLE 1 (1) Test against rice blast/ (Piricularia oryzae) (pot test) Paddy rice (Jukkoku variety) was cultivated in pots of 12 cm. in diameter and the diluted aqueous solution of the particular active compound in the formulation of wettable powder as described in Formulation A was sprayed on the rice plants at their young ear forming stage until leaves of rice plants became dripping wet. On the next day the sprayed (i.e. treated) rice plants were placed in a moisture chamber and kept there under conditions of the relative humidity of 100% at the temperature of 25 C. for 4 8 hours. During that time a spore suspension of rice blast (Piriculariae oryzae) pathogen was sprayed onto two times for inoculation. After the inoculated rice plants were kept under such conditions for 7 days, the disease attack rate, i.e. infestation, per pot was evaluated and classified according to the rating from 0 to 5, and the controlling value against blast was calculated from the following formula:

Disease attack rate Percentage of disease-.

Controlling value Infestation in non-treated plot-I. in treated plot Infestation in non-treated plot TABLE 1.-TEST RESULTS OF FUNGICIDAL EFFECT AGAINST RICE BLAST [Pot test] 1 Known compound-comparison.

Nora-Compounds of invention have corresponding numbers to those of Table 3 and Example 3 below, as the case may be.

EXAMPLE 2 Test against plant pathogens (agar dilution method) The particular active compound is mixed in an agar culture medium of potato to form the desired concentration of active compound therein. After the medium is poured into Petri dishes of 9 cm. in diameter and coagulated, the same are inoculated with the corresponding plant pathogens. Standard Petri dishes to which the active compound of Zineb (Zine-ethylene-bis-dithiocarbamate) preparation are added are also set up. After having been cultured at 27 C. for 4 days, the growth condition of the plant pathogens is investigated and the minimum concentration of the active compound (in p.p.m.) for growth inhibition is determined.

The particular active compounds tested and the results obtained (i.e. the minimum concentration in p.p.m. for growth inhibition) can be seen from the following Table 2.

TABLE 2.TEST RESULT OF FUNGICIDAL EFFECT AGAINST VARIOUS PLANT PATHOGENS [Agar dilution method in p.p.m.]

Piricu- Pellicu- Elsinoe Active laria Cochlz'obolus laria Alternan'a ampeoompound ory zae miyabeanus sasakii lcikuchiana line No. (rice) (rice) (rice) (pear) (grape) (standard). 50 200 100 200 200 Norm-Compounds of invention have corresponding numbers to those of Table 3 and Example 3 below, as the case may be.

The following further examples illustrate, without limitation, the process for producing the particular new compounds of the present invention.

EXAMPLE 3 0 S-OzHs O (Hi-n 3) 11 g. of thiophenol and 10 g. of triethylamine are dissolved in 200 ml. of benzene. To this solution, which is maintained at a temperature below 10 C., 22 g. of O-nbutyl-S-ethyl-thiolphosphoryl chloride (B.P. C./0.1 mm. Hg) is added dropwise. After the addition, the mixture is stirred for 1 hour at the room temperature and stirred further for 4 hours at a temperature of 60 C. to complete the reaction. The organic layer is washed by water and then with 1% aqueous solution of sodium carbonate and water, and thereafter dehydrated over anhydrous sodium sulfate. Upon distilling ofI' the attendant benzene and then distilling the residue further, 19 g. of colorless oily O-n-butyl-S-ethyl-S-phenyl-phosphorodithiolate, B.P. 152--157 C./0.1 mm. Hg, is obtained.

According to the same procedure, when O-n-butyl-S- sec.-butyl-thiolphosphoryl chloride, O-n-hexyl-S-ethylthiolphosphoryl chloride, O-iso-propyl-S-ethyl-thiolphosphoryl chloride and O-ethyl-S-methyl-thiolphosphoryl chloride are used, respectively, instead of O-n-butyl-S- ethyl-thiolphosphoryl chloride, the corresponding O-alkyl- S-ethyl-S-phenyl-phosphorodithiolates which have the similar fungicidal activity are obtained, i.e.:

(1 1 O-n-butyl-SPsec.-butyl-S-phenyl-phosphorodithiolate (12 O-n-hexyl-S-ethyl-S-phenyl-phosphorodithiolate 13 O-isopropyl S-ethyl-S-phenyl-phosphorodithiolate (14 O-ethyl-S-methyl-S-phenyl-phosphorodithiolate EXAMPLE 4 5.5 g. of thiophenol and 5 g. of triethylamine are dissolved in ml. of benzene. To this solution, 12.1 g. of O-cyclohexyl-S-ethyl-thiolphosphoryl chloride (B.P. 112 C./0.6 mm. Hg) is added dropwise while cooling, and the mixture is stirred for 3 hours at a temperature of 70 C. After the reacted mixture becomes cool, the organic layer is washed with water and then with 1% aqueous solution of sodium carbonate and water. The washed organic layer is thereafter dehydrated over anhydrous sodium sulfate. Upon distilling off the benzene present, 12 g. of pale yellow oily O-cyclohexyl-S-ethyl-S phenylphosphorodithiolate are obtained as residue. This product is nondistillable at C./0.1 mm. Hg.

According to the same procedure, when O-cyclohexyl- S-n-butyl-thiolphosphoryl chloride is used instead of O- cyclohexyl-S-ethyl-thiolphosphoryl chloride, the pale yellow oily product, 0-cyclohexyl-S-n-butyl-S-phenylphosphorodithiolate (15 which has the similar fungicidal activity, is obtained. This is nondistillable at 160 C./0.1 mm. Hg.

The following Table 3 illustrates appropriate data for typical compounds of the present invention.

TABLE 3 Compound Structural formula Physical properties (13) s-oH, B.P.149152 0.10.1 mm. Hg.

v 0-O4H1l-n (2 O SCHQ B.P. 153-458 C./0.02 mm. Hg.

ClS-l I 0' 4Hin (34) O S-CZHI B.P. 152-157" 0.10.! mm. Hg.

0C4HD-n (4a)....'....'.' 0 S-CaHs B.P. 159-165" 0.10.02 mm. Hg.

Cl-'S-l OC4Ho-n (5 O S--C3H5 B.P. 155156 C./0.1 mm. Hg.

GHQ-S-I 0-CH9n (6;) 0 S-C'Hg (7213 1.5740) oil.

(7;) O S-CH; (1113 1.5855) oil.

C1-Sl (84) s :Il(i/SCzH (M3 1.5640) 011.

o1-s-i (10:) O S-CzHs 011.

These compounds may be designated:

It will be realized by the artisan that all of the foregoing compounds contemplated by the present invention possess the desired strong fungicidal properties, with regard to a broad spectrum of activity, as well as a comparatively low toxicity toward warm-blooded creatures and a concomitantly low phytotoxicity, enabling such compounds to be used with correspondingly favorable compatibility with warm-blooded creatures and plants for more effective control and/or elimination of fungi by application of such compounds to such fungi and/ or their habitat.

It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.

What is claimed is:

1. Phosphorodithiolate of the formula in which R is alkyl of 1-4 carbon atoms, R' is selected from the group consisting of straight chain alkyl of 4-6 carbon atoms and cyclohexyl, and X is selected from the group consisting of hydrogen, chloro and methyl.

2. Compound according to claim 1 wherein R is 0 alkyl, R is cyclohexyl, and X is selected from the group consisting of hydrogen, chloro and methyl.

1 1 3. Compound according to claim 1 wherein such compound is O-n-butyl-SFmethy1-S-phenyl-phosphorodithiolate of the formula 4. Compound according to claim 1 wherein such compound is O n-butyl-S-methyl-S-(4-chloro-phenyl)-phosphorodithiolate of the formula O-GAHp-ll 5. Compound according to claim 1 wherein such compound is O n-butyl-Sethyl-S-phenyl-phosphorodithiolate of the formula 6. Compound according to claim 1 wherein such compound is O n butyl-S-ethyl-S-(4-chloro-phenyl)-phosphorodithiolate of the formula 7. Compound according to claim 1 wherein such compound is O n butyl-S-ethyl-S-(4-methyl-phenyl)-phosphorodithiolate of the formula CE SA 8. Compound according to claim 1 wherein such com- 12 pound is 0 cyclohexyl S-methyl-S-(4-ch1oro-phenyl)- phosphorodithiolate of the formula 9. Compound according to claim 1 wherein such compound is O-cyclohexyl-S-ethyl-S-phenyl-phosphorodithiolate of the formula 11. Compound according to claim 1 wherein such compound is O cyclohexyl-S-methyl-S-phenyl-phosphorodithiolate of the formula 0 S-CH:

References Cited FOREIGN PATENTS 98,101 2/1964 Denmark 260-964 1,288,843 i 2/1969 Germany 260-958 ANTON H. SUTI'O, Primary Examiner US. Cl. X.R.

" (233? UNITED STATES-PATENT OFFICE CERTIFICATE OF CORRECTIQN j v Patent No. 3,784,554 I I I Dated January 8 1974 I 1npvencor(s) Teyoh i ko Kume et al I i It is certified that: error appears 5 in the aboyeidefltified patent. and that said Letters Patent are hereby corrected as shown below:

E1. 4, l in e"3, cosi'ect spelling oF'BasidiOmycetes".

Col. 8, Example 4 111 the formula, change '0- to O- G01; 9, Table 3, Compound (3 in the formula, change -(2 H Gal, 1]., Claimfi, inthe formula, change "S1" to S Col. 12, Claim 8, 1n the: formula, before "CH change "0" to -S-.

Signed and sealed this 27th day of August 1974.

(SEAL) Attest:

MCCOY M. GIBSON, JR; ,c. MARSEIALL DANN Attesting Officer Commlssloner of Patents 

